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通过原子力显微镜测量的单细胞复剪切模量的数值分布。

The number distribution of complex shear modulus of single cells measured by atomic force microscopy.

作者信息

Hiratsuka Shinichiro, Mizutani Yusuke, Tsuchiya Masahiro, Kawahara Koichi, Tokumoto Hiroshi, Okajima Takaharu

机构信息

Graduate School of Information Science and Technology, Hokkaido University, Kita-ku N14 W9, Sapporo 060-0814, Japan.

出版信息

Ultramicroscopy. 2009 Jul;109(8):937-41. doi: 10.1016/j.ultramic.2009.03.008. Epub 2009 Mar 19.

Abstract

The viscoelastic properties of a large number of mouse fibroblast NIH3T3 cells (n approximately 130) were investigated by combining atomic force microscopy (AFM) with a microarray technique. In the experiments, the cells were arranged and cultured in the wells of a microarray substrate, and a force modulation mode experiment was used to measure the complex shear modulus, G*, of individual cells in a frequency range 0.5-200Hz. The frequency dependence of G* of the cells exhibited a power-law behavior and similar frequency dependencies have been observed in several cell types cultured on flat substrates. This indicated that the NIH3T3 cells cultured in the wells of a microarray have analogous structural organization to those cells cultured on flat substrates. The number distribution of both the storage and loss moduli of G* fitted well to a log-normal distribution function, whereas the power-law exponent estimated by a power-law structural damping model showed a normal distribution function. These results showed that combining AFM with a microarray technique was a suitable approach for investigating the statistics of rheological properties of living cells without the requirement of cell surface modification.

摘要

通过将原子力显微镜(AFM)与微阵列技术相结合,研究了大量小鼠成纤维细胞NIH3T3(约130个)的粘弹性特性。在实验中,将细胞排列并培养在微阵列基板的孔中,并使用力调制模式实验在0.5-200Hz频率范围内测量单个细胞的复剪切模量G*。细胞G的频率依赖性表现出幂律行为,并且在培养于平坦基板上的几种细胞类型中也观察到了类似的频率依赖性。这表明在微阵列孔中培养的NIH3T3细胞与在平坦基板上培养的细胞具有类似的结构组织。G的储能模量和损耗模量的数量分布都很好地拟合了对数正态分布函数,而由幂律结构阻尼模型估计的幂律指数显示为正态分布函数。这些结果表明,将AFM与微阵列技术相结合是一种适用于研究活细胞流变学特性统计而无需细胞表面修饰的方法。

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